Aromatic Hydrocarbon
CHXI13:HYDROCARBONS

318232 Anhydrous \(\mathrm{AlCl}_{3}\) is used as a catalyst in the Friedel-Crafts reaction because it is

1 an electron-rich molecule
2 soluble in ether
3 ionisable to \(\mathrm{Al}^{3+}\) and \(\mathrm{Cl}^{-}\)
4 an electron-deficient molecule
CHXI13:HYDROCARBONS

318233 Assertion :
In nitration, \(\mathrm{H}_{2} \mathrm{SO}_{4}\) is used as nitronium ion producer.
Reason :
Benzene has multi center \(\pi\) bonding.

1 Both Assertion and Reason are correct and Reason is the correct explanation of the Assertion.
2 Both Assertion and Reason are correct but Reason is not the correct explanation of the Assertion.
3 Assertion is correct but Reason is incorrect.
4 Assertion is incorrect but Reason is correct.
CHXI13:HYDROCARBONS

318234 Benzene reacts with sulphuric acid to form benzenesulphonic acid, only when the sulphuric acid is

1 cold and dilute
2 hot and dilute
3 hot and concentrated
4 mixed with \(\mathrm{HNO}_{3}\)
CHXI13:HYDROCARBONS

318235 Decreasing order of reactivity toward electrophilic substitution for the following compounds is
supporting img

1 D \(>\) A \(>\) E \(>\) C \(>\) B
2 A \(>\) D \(>\) E \(>\) B \(>\) C
3 C \(>\) B \(>\) A \(>\) D \(>\) E
4 E \(>\) D \(>\) A \(>\) B \(>\) C
CHXI13:HYDROCARBONS

318232 Anhydrous \(\mathrm{AlCl}_{3}\) is used as a catalyst in the Friedel-Crafts reaction because it is

1 an electron-rich molecule
2 soluble in ether
3 ionisable to \(\mathrm{Al}^{3+}\) and \(\mathrm{Cl}^{-}\)
4 an electron-deficient molecule
CHXI13:HYDROCARBONS

318233 Assertion :
In nitration, \(\mathrm{H}_{2} \mathrm{SO}_{4}\) is used as nitronium ion producer.
Reason :
Benzene has multi center \(\pi\) bonding.

1 Both Assertion and Reason are correct and Reason is the correct explanation of the Assertion.
2 Both Assertion and Reason are correct but Reason is not the correct explanation of the Assertion.
3 Assertion is correct but Reason is incorrect.
4 Assertion is incorrect but Reason is correct.
CHXI13:HYDROCARBONS

318234 Benzene reacts with sulphuric acid to form benzenesulphonic acid, only when the sulphuric acid is

1 cold and dilute
2 hot and dilute
3 hot and concentrated
4 mixed with \(\mathrm{HNO}_{3}\)
CHXI13:HYDROCARBONS

318235 Decreasing order of reactivity toward electrophilic substitution for the following compounds is
supporting img

1 D \(>\) A \(>\) E \(>\) C \(>\) B
2 A \(>\) D \(>\) E \(>\) B \(>\) C
3 C \(>\) B \(>\) A \(>\) D \(>\) E
4 E \(>\) D \(>\) A \(>\) B \(>\) C
CHXI13:HYDROCARBONS

318232 Anhydrous \(\mathrm{AlCl}_{3}\) is used as a catalyst in the Friedel-Crafts reaction because it is

1 an electron-rich molecule
2 soluble in ether
3 ionisable to \(\mathrm{Al}^{3+}\) and \(\mathrm{Cl}^{-}\)
4 an electron-deficient molecule
CHXI13:HYDROCARBONS

318233 Assertion :
In nitration, \(\mathrm{H}_{2} \mathrm{SO}_{4}\) is used as nitronium ion producer.
Reason :
Benzene has multi center \(\pi\) bonding.

1 Both Assertion and Reason are correct and Reason is the correct explanation of the Assertion.
2 Both Assertion and Reason are correct but Reason is not the correct explanation of the Assertion.
3 Assertion is correct but Reason is incorrect.
4 Assertion is incorrect but Reason is correct.
CHXI13:HYDROCARBONS

318234 Benzene reacts with sulphuric acid to form benzenesulphonic acid, only when the sulphuric acid is

1 cold and dilute
2 hot and dilute
3 hot and concentrated
4 mixed with \(\mathrm{HNO}_{3}\)
CHXI13:HYDROCARBONS

318235 Decreasing order of reactivity toward electrophilic substitution for the following compounds is
supporting img

1 D \(>\) A \(>\) E \(>\) C \(>\) B
2 A \(>\) D \(>\) E \(>\) B \(>\) C
3 C \(>\) B \(>\) A \(>\) D \(>\) E
4 E \(>\) D \(>\) A \(>\) B \(>\) C
CHXI13:HYDROCARBONS

318232 Anhydrous \(\mathrm{AlCl}_{3}\) is used as a catalyst in the Friedel-Crafts reaction because it is

1 an electron-rich molecule
2 soluble in ether
3 ionisable to \(\mathrm{Al}^{3+}\) and \(\mathrm{Cl}^{-}\)
4 an electron-deficient molecule
CHXI13:HYDROCARBONS

318233 Assertion :
In nitration, \(\mathrm{H}_{2} \mathrm{SO}_{4}\) is used as nitronium ion producer.
Reason :
Benzene has multi center \(\pi\) bonding.

1 Both Assertion and Reason are correct and Reason is the correct explanation of the Assertion.
2 Both Assertion and Reason are correct but Reason is not the correct explanation of the Assertion.
3 Assertion is correct but Reason is incorrect.
4 Assertion is incorrect but Reason is correct.
CHXI13:HYDROCARBONS

318234 Benzene reacts with sulphuric acid to form benzenesulphonic acid, only when the sulphuric acid is

1 cold and dilute
2 hot and dilute
3 hot and concentrated
4 mixed with \(\mathrm{HNO}_{3}\)
CHXI13:HYDROCARBONS

318235 Decreasing order of reactivity toward electrophilic substitution for the following compounds is
supporting img

1 D \(>\) A \(>\) E \(>\) C \(>\) B
2 A \(>\) D \(>\) E \(>\) B \(>\) C
3 C \(>\) B \(>\) A \(>\) D \(>\) E
4 E \(>\) D \(>\) A \(>\) B \(>\) C
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